Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome. 24129430 2014
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome). 22315194 2012
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome. 22228761 2012
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum. 21739589 2011
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. 20802478 2010
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		0.800 GeneticVariation UNIPROT Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. 20802478 2010
dbSNP: rs267606951
rs267606951
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		0.800 GeneticVariation UNIPROT Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. 20802478 2010
dbSNP: rs267606952
rs267606952
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		0.800 GeneticVariation UNIPROT Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. 20802478 2010
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		T 0.800 CausalMutation CLINVAR
dbSNP: rs267606951
rs267606951
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		C 0.800 CausalMutation CLINVAR
dbSNP: rs267606952
rs267606952
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C4551502
Disease:
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 		A 0.800 CausalMutation CLINVAR
dbSNP: rs112535818
rs112535818
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0018498
Disease:
Hair Color 		G 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018
dbSNP: rs146091102
rs146091102
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0200633
Disease:
Neutrophil count (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs146091102
rs146091102
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1855923
Disease:
Hyperphosphatasia with Mental Retardation 		A 0.700 GeneticVariation CLINVAR Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome. 24129430 2014
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1855923
Disease:
Hyperphosphatasia with Mental Retardation 		A 0.700 GeneticVariation CLINVAR Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome). 22315194 2012
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1855923
Disease:
Hyperphosphatasia with Mental Retardation 		A 0.700 GeneticVariation CLINVAR Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome. 22228761 2012
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1855923
Disease:
Hyperphosphatasia with Mental Retardation 		A 0.700 GeneticVariation CLINVAR Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum. 21739589 2011
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1855923
Disease:
Hyperphosphatasia with Mental Retardation 		A 0.700 GeneticVariation CLINVAR Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. 20802478 2010
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1865014
Disease:
Long philtrum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1865017
Disease:
Thin upper lip vermilion 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0036572
Disease:
Seizures 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0423109
Disease:
Upward slant of palpebral fissure 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C0557874
Disease:
Global developmental delay 		A 0.700 CausalMutation CLINVAR
dbSNP: rs139073416
rs139073416
Entrez Id: 55650
Gene Symbol: PIGV
PIGV
CUI: C1314665
Disease:
Serum alkaline phosphatase raised 		A 0.700 CausalMutation CLINVAR